Home
Class 12
CHEMISTRY
Statement-I: Aryl halidea undergo electr...

Statement-I: Aryl halidea undergo electrophilic substitution less radily than benzene.
Because Statement-II: Ary, halide gives only meta product w.r.t. electrophilic substitution.

A

Statement-I is True, Statement-II is True, Statement-II is a correct explanation for Statement-I

B

Statement-I is True, Statement-II is True, Statement-II is NOT a correct explanation for Statement-I

C

Statement-I is True, Statement-II is False.

D

Statement-I is False, Statement-II is True.

Text Solution

Verified by Experts

The correct Answer is:
C
Promotional Banner

Similar Questions

Explore conceptually related problems

Statement-I: Vinylic halides are reactive towards nucleophilic substitution reaction. Because Statement-II: Reactivity is due to the polarity of carbon-halogen bond.

Statement-I: Optically active 2-idoibutane on treatment with NaI in acetone undergoes racemisation. Because Statement-II: Repeated Walden inversions on the reactant and its product evantually gives a racemic mixure.

Statement-I:Primay benzylic halides are more reactive than primary alkyl halides towards S_(N^(1)) reaction. Because Statement-II: Reactivity depends upon the nature of the nucleophile and the solvent.

Statement-I: Polar solvent slows down S_(N^(2)) reaction. Because Statement-II: CH_(3)-Br is less reactive than CH_(3)CI .

Statement-I: If an aqueous solution of NaCI is electrolysed, the product obtained at the cathode is H_(2) gas and no Na. Because Statement-II: Gases are liberated faster than the metals.

Statement-I: Free radical chlorination of n-butane gives 72% of 2-chlorobutane and 28% of 1-chlorobutane though it has six primary and four secondary hydrogens. Because Statement-II: A secondary hydrogen is abstracted more easily than the primary hydrogen.